54557-81-2

Usage

Uses

Due to the limited information available on the specific uses, sources, and preparation of 4-[3,4-(Ethylendioxy)phenyl]-4-oxobutyric Acid, it is not possible to provide a detailed list of its applications. However, given its chemical structure and classification, it may have potential applications in various industries, such as pharmaceuticals, agrochemicals, or materials science, where similar compounds are utilized. Further research and development would be required to explore and confirm its practical applications.

InChI:InChI=1/C12H12O5/c13-9(2-4-12(14)15)8-1-3-10-11(7-8)17-6-5-16-10/h1,3,7H,2,4-6H2,(H,14,15)

Upstream product

• 108-30-5 succinic acid anhydride 
• 493-09-4 benzo-1,4-dioxane 
• 951889-31-9 4-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-4-oxo-butyric acid ethyl ester 

Downstream Products

• 860689-19-6 5-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-dihydro-furan-2-one 
• 951889-31-9 4-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-4-oxo-butyric acid ethyl ester 

Relevant academic research and scientific papers

An Electrophilic Trifluoromethylthiolation of Silylenol Ethers and β-Naphthols with Diethylaminosulfur Trifluoride and (Trifluoromethyl)trimethylsilane

An efficient and general trifluoromethylthiolation of silylenol ethers and β-naphthols have been accomplished employing the combination of diethylaminosulfur trifluoride (DAST) and (trifluoromethyl)trimethylsilane (CF3TMS) as source of electrophilic trifluoromethylthio moiety for the synthesis of α-trifluoromethylthiolated carbonyl compounds and β-naphthols in good yields. Important features of this method include wide functional group tolerance and use of readily available DAST/CF3TMS. Potential of the methodology was demonstrated via the synthesis of α-trifluoromethylthiolated (+)-4-cholesten-3-one and naphthoquinone. (Figure presented.).

Synthesis and biological activity of new anti-inflammatory compounds containing the 1,4-benzodioxine and/or pyrrole system

A series of substituted derivatives containing the 1,4-benzodioxine or pyrrole nucleus are described. All the newly synthesized compounds were examined for their in vitro and in vivo anti-inflammatory activity. Several derivatives, including (S)-2, 14 and 17, showed more anti-inflammatory activity in vivo in these assays (rat paw oedema induced by carrageenan) than the known classical anti-inflammatory agent ibuprofen, whereas other compounds like 1 were equipotent to ibuprofen. Compound 17 was the most outstanding derivative because of its remarkable in vivo anti-inflammatory activity. In this paper, we examine and discuss the structure-activity relationships and anti-inflammatory activities of these compounds.